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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:19685247


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:20358615, PMID:7747785


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:10767004, PMID:18423521


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:25590586


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:19764023, PMID:20358615, PMID:21204207, PMID:23578821, PMID:25590586, PMID:25741868, PMID:7747785


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:10767004, PMID:18423521, PMID:20358615, PMID:25590586, PMID:25741868


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Tfap2a and branchiooculofacial syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TFAP2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to branchiooculofacial syndrome  (DOID:0050691)
  • 18 papers in RGD have been used to annotate Tfap2a
  • Curation Notes: ClinVar Annotator: match by term: Branchiooculofacial syndrome


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.